Canonical Allele Identifier: CA1941711362

Gene: ACADSB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.123034684_123034689delinsGTCTAC , CM000672.2:g.123034684_123034689delinsGTCTAC	GRCh38
NC_000010.10:g.124794200_124794205delinsGTCTAC , CM000672.1:g.124794200_124794205delinsGTCTAC	GRCh37
NC_000010.9:g.124784190_124784195delinsGTCTAC	NCBI36
NG_008003.1:g.30772_30777delinsGTCTAC , LRG_451:g.30772_30777delinsGTCTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358776.7:c.202+169_202+174delinsGTCTAC MANE Select	ENSP00000357873.3:n.202+169_202+174delinsGTCTAC
ENST00000358776.6:c.202+169_202+174delinsGTCTAC	ENSP00000357873.3:n.202+169_202+174delinsGTCTAC
ENST00000368869.8:c.-4+169_-4+174delinsGTCTAC	ENSP00000357862.4:n.-4+169_-4+174delinsGTCTAC
ENST00000411816.2:n.219+169_219+174delinsGTCTAC
NM_001609.3:c.202+169_202+174delinsGTCTAC , LRG_451t1:c.202+169_202+174delinsGTCTAC	NP_001600.1:n.202+169_202+174delinsGTCTAC
NM_001330174.1:c.-4+169_-4+174delinsGTCTAC	NP_001317103.1:n.-4+169_-4+174delinsGTCTAC
NM_001330174.2:c.-4+169_-4+174delinsGTCTAC	NP_001317103.1:n.-4+169_-4+174delinsGTCTAC
NM_001609.4:c.202+169_202+174delinsGTCTAC MANE Select	NP_001600.1:n.202+169_202+174delinsGTCTAC
NM_001330174.3:c.-4+169_-4+174delinsGTCTAC	NP_001317103.1:n.-4+169_-4+174delinsGTCTAC